Secondary hypertension due to a juxtaglomerular cell tumor

被引:10
|
作者
Nunes, Igor [1 ]
Santos, Tiago [1 ]
Tavares, Joana [2 ]
Correia, Lurdes [2 ]
Coutinho, Joao [3 ]
Nogueira, J. M. Braz [1 ]
Carvalho, Leonor [1 ]
Soares, J. L. Ducla [1 ]
机构
[1] Ctr Hosp Lisboa Norte, Hosp Santa Maria, Internal Med Dept 1, Lisbon Med Fac, Lisbon, Portugal
[2] Ctr Hosp Lisboa Norte, Hosp Santa Maria, Clin Pathol Dept, Lisbon Med Fac, Lisbon, Portugal
[3] Ctr Hosp Lisboa Norte, Hosp Santa Maria, Clin Pathol Dept, Gen Surg Dept, Lisbon, Portugal
关键词
Hypertension; juxtaglomerular cell tumor; plasma renin activity; renin-secreting tumor;
D O I
10.1016/j.jash.2018.05.005
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Juxtaglomerular cell tumors are rare, generally benign, and they are one of the secondary surgically treatable causes of arterial hypertension. There are about 100 reported cases on literature, and the diagnosis is usually carried out based on a high clinic suspicion index, mostly in patients with hypokalemia and arterial hypertension. The diagnosis involves blood tests and imaging studies, but it is only definite with histopathological exam after surgical treatment. We present a case of a 22-year-old woman with resistant arterial hypertension and renal and cardiovascular target-organ lesions. High plasmatic renin and a nodular renal mass on magnetic resonance imaging were present. A tumorectomy was performed and the histological exam confirmed a reninoma. After surgery, blood pressure and serum renin values returned to normal without medication. This work focuses on the need to exclude rare secondary causes of hypertension in young patients with resistant forms of this disease. (C) 2018 American Heart Association. All rights reserved.
引用
收藏
页码:637 / 640
页数:4
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